Superoxide dismutase in aging and disease: an overview (Q34576334)

3 August 2017

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title

Superoxide dismutase in aging and disease: an overview (English)

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3 August 2017

Joe M McCord

1

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3 August 2017

language of work or name

English

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publication date

1 January 2002

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3 August 2017

published in

Methods in Enzymology

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3 August 2017

volume

349

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3 August 2017

page(s)

331-341

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Interstitial equilibration of superoxide dismutase correlates with its protective effect in the isolated rabbit heart

3 August 2017

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Cardioprotection by Cu,Zn-superoxide dismutase is lost at high doses in the reoxygenated heart

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The toxicity of high-dose superoxide dismutase suggests that superoxide can both initiate and terminate lipid peroxidation in the reperfused heart

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Exercise provides direct biphasic cardioprotection via manganese superoxide dismutase activation

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Iron mobilization from ferritin by superoxide derived from stimulated polymorphonuclear leukocytes. Possible mechanism in inflammation diseases

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Biologically relevant metal ion-dependent hydroxyl radical generation. An update

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Iron-load increases the susceptibility of rat hearts to oxygen reperfusion damage. Protection by the antioxidant ( )-cyanidanol-3 and deferoxamine

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Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

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Extracellular superoxide dismutase deficiency worsens outcome from focal cerebral ischemia in the mouse

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Enhanced alloxan-induced beta-cell damage and delayed recovery from hyperglycemia in mice lacking extracellular-superoxide dismutase

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Mutations in the promoter reveal a cause for the reduced expression of the human manganese superoxide dismutase gene in cancer cells.

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Tumor Necrosis Factor Alpha and Interleukin-1β Regulate the Murine Manganese Superoxide Dismutase Gene Through a Complex Intronic Enhancer Involving C/EBP-β and NF-κB

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Identifiers

DOI

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3 August 2017

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